BRPI0415421A - sulfoximine-substituted pyrimidines as cdk and / or vegf inhibitors, their preparation and their use as a medicament - Google Patents
sulfoximine-substituted pyrimidines as cdk and / or vegf inhibitors, their preparation and their use as a medicamentInfo
- Publication number
- BRPI0415421A BRPI0415421A BRPI0415421-5A BRPI0415421A BRPI0415421A BR PI0415421 A BRPI0415421 A BR PI0415421A BR PI0415421 A BRPI0415421 A BR PI0415421A BR PI0415421 A BRPI0415421 A BR PI0415421A
- Authority
- BR
- Brazil
- Prior art keywords
- preparation
- cdk
- substituted pyrimidines
- sulfoximine
- medicament
- Prior art date
Links
- 239000003814 drug Substances 0.000 title abstract 3
- 150000003230 pyrimidines Chemical class 0.000 title abstract 3
- 239000002525 vasculotropin inhibitor Substances 0.000 title abstract 2
- 229940122560 Cyclin inhibitor Drugs 0.000 abstract 1
- 108091000080 Phosphotransferase Proteins 0.000 abstract 1
- 102000004278 Receptor Protein-Tyrosine Kinases Human genes 0.000 abstract 1
- 108090000873 Receptor Protein-Tyrosine Kinases Proteins 0.000 abstract 1
- 102000005789 Vascular Endothelial Growth Factors Human genes 0.000 abstract 1
- 108010019530 Vascular Endothelial Growth Factors Proteins 0.000 abstract 1
- 230000001419 dependent effect Effects 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 229940079593 drug Drugs 0.000 abstract 1
- 102000020233 phosphotransferase Human genes 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
- C07D239/47—One nitrogen atom and one oxygen or sulfur atom, e.g. cytosine
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
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- A—HUMAN NECESSITIES
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- A—HUMAN NECESSITIES
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- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
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- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
- C07D239/48—Two nitrogen atoms
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
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- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Virology (AREA)
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- Urology & Nephrology (AREA)
- Cardiology (AREA)
- Tropical Medicine & Parasitology (AREA)
- Psychology (AREA)
- Psychiatry (AREA)
- Gastroenterology & Hepatology (AREA)
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Abstract
"PIRIMIDINAS SUBSTITUìDAS POR SULFóXIMINA COMO INIBIDORES DE CDK E/OU VEGF, SUA PREPARAçãO E SEU EMPREGO COMO MEDICAMENTO". Da presente invenção refere-se a um derivado de pirimidina de acordo com a fórmula I na qual o Q, R¬ 1¬, R¬ 2¬, R¬ 3¬, R¬ 4¬, R¬ 5¬, X, e m têm os significados contidos na descrições como cinases dependentes de inibidores de ciclina e receptores de tirosina quinase VEGF, cuja preparação assim como seu emprego como medicamento para tratamento de diversas doenças."Sulfoxime-Substituted Pyrimidines as CDK and / or VEGF Inhibitors, Their Preparation and Employment as a Drug". The present invention relates to a pyrimidine derivative according to formula I wherein Q, R¬1¬, R¬2¬, R¬3¬, R¬4¬, R¬5¬, X, have the meanings contained in the descriptions as cyclin inhibitor dependent kinases and VEGF tyrosine kinase receptors, the preparation of which as well as their use as a medicine for the treatment of various diseases.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE10349423A DE10349423A1 (en) | 2003-10-16 | 2003-10-16 | Sulfoximine-substituted parimidines as CDK and / or VEGF inhibitors, their preparation and use as medicaments |
| PCT/EP2004/011661 WO2005037800A1 (en) | 2003-10-16 | 2004-10-12 | Sulfoximine-substituted pyrimidines for use as cdk and/or vegf inhibitors, the production thereof and their use as drugs |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| BRPI0415421A true BRPI0415421A (en) | 2006-12-05 |
Family
ID=34442222
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BRPI0415421-5A BRPI0415421A (en) | 2003-10-16 | 2004-10-12 | sulfoximine-substituted pyrimidines as cdk and / or vegf inhibitors, their preparation and their use as a medicament |
Country Status (35)
| Country | Link |
|---|---|
| US (2) | US8507510B2 (en) |
| EP (1) | EP1673352B1 (en) |
| JP (1) | JP4700006B2 (en) |
| KR (1) | KR101117387B1 (en) |
| CN (1) | CN1867553B (en) |
| AR (1) | AR046119A1 (en) |
| AT (1) | ATE427939T1 (en) |
| AU (1) | AU2004281960B2 (en) |
| BR (1) | BRPI0415421A (en) |
| CA (1) | CA2542492C (en) |
| CR (1) | CR8363A (en) |
| CY (1) | CY1110058T1 (en) |
| DE (2) | DE10349423A1 (en) |
| DK (1) | DK1673352T3 (en) |
| EC (1) | ECSP066568A (en) |
| ES (1) | ES2324475T3 (en) |
| GT (1) | GT200400206A (en) |
| HR (1) | HRP20090348T1 (en) |
| IL (1) | IL174952A (en) |
| JO (1) | JO2534B1 (en) |
| ME (1) | ME00158B (en) |
| MX (1) | MXPA06004091A (en) |
| MY (1) | MY140291A (en) |
| NO (1) | NO337290B1 (en) |
| NZ (1) | NZ546510A (en) |
| PE (1) | PE20050907A1 (en) |
| PL (1) | PL1673352T3 (en) |
| PT (1) | PT1673352E (en) |
| RS (1) | RS51657B (en) |
| RU (1) | RU2410378C2 (en) |
| SI (1) | SI1673352T1 (en) |
| TW (1) | TWI347844B (en) |
| UA (1) | UA86041C2 (en) |
| WO (1) | WO2005037800A1 (en) |
| ZA (1) | ZA200603885B (en) |
Families Citing this family (96)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR100874791B1 (en) * | 2001-05-29 | 2008-12-18 | 바이엘 쉐링 파마 악티엔게젤샤프트 | CDV-inhibited pyrimidine, preparation method thereof and use as medicament |
| TWI329105B (en) | 2002-02-01 | 2010-08-21 | Rigel Pharmaceuticals Inc | 2,4-pyrimidinediamine compounds and their uses |
| GB0205688D0 (en) | 2002-03-09 | 2002-04-24 | Astrazeneca Ab | Chemical compounds |
| GB0205690D0 (en) | 2002-03-09 | 2002-04-24 | Astrazeneca Ab | Chemical compounds |
| GB0205693D0 (en) | 2002-03-09 | 2002-04-24 | Astrazeneca Ab | Chemical compounds |
| US7442697B2 (en) | 2002-03-09 | 2008-10-28 | Astrazeneca Ab | 4-imidazolyl substituted pyrimidine derivatives with CDK inhibitory activity |
| ES2445208T3 (en) | 2002-07-29 | 2014-02-28 | Rigel Pharmaceuticals, Inc. | 2,4-Pyrimidinediamine compounds for use in methods to treat or prevent autoimmune diseases |
| US7157455B2 (en) | 2003-02-10 | 2007-01-02 | Hoffmann-La Roche Inc. | 4-Aminopyrimidine-5-one derivatives |
| GB0311276D0 (en) | 2003-05-16 | 2003-06-18 | Astrazeneca Ab | Chemical compounds |
| GB0311274D0 (en) | 2003-05-16 | 2003-06-18 | Astrazeneca Ab | Chemical compounds |
| BRPI0413018B8 (en) | 2003-07-30 | 2021-05-25 | Rigel Pharmaceuticals Inc | compost, and use of a compost |
| DE10349423A1 (en) * | 2003-10-16 | 2005-06-16 | Schering Ag | Sulfoximine-substituted parimidines as CDK and / or VEGF inhibitors, their preparation and use as medicaments |
| EP1763514A2 (en) | 2004-05-18 | 2007-03-21 | Rigel Pharmaceuticals, Inc. | Cycloalkyl substituted pyrimidinediamine compounds and their uses |
| GB2420559B (en) | 2004-11-15 | 2008-08-06 | Rigel Pharmaceuticals Inc | Stereoisomerically enriched 3-aminocarbonyl bicycloheptene pyrimidinediamine compounds and their uses |
| DE602006010979D1 (en) | 2005-01-19 | 2010-01-21 | Rigel Pharmaceuticals Inc | PRODRUGS FROM 2,4-PYRIMIDIN DIAMIN COMPOUNDS AND THEIR USES |
| EP1705177A1 (en) * | 2005-03-23 | 2006-09-27 | Schering Aktiengesellschaft | N-aryl-sulfoximine-substituted pyrimidines as CDK- and/or VEGF inhibitors, their production and use as pharmaceutical agents |
| EP1710246A1 (en) * | 2005-04-08 | 2006-10-11 | Schering Aktiengesellschaft | Sulfoximine-pyrimidine Macrocycles and the salts thereof, a process for making them, and their pharmaceutical use against cancer |
| US20070203161A1 (en) * | 2006-02-24 | 2007-08-30 | Rigel Pharmaceuticals, Inc. | Compositions and methods for inhibition of the jak pathway |
| WO2006133426A2 (en) | 2005-06-08 | 2006-12-14 | Rigel Pharmaceuticals, Inc. | Compositions and methods for inhibition of the jak pathway |
| EP1928437A2 (en) | 2005-08-26 | 2008-06-11 | Braincells, Inc. | Neurogenesis by muscarinic receptor modulation |
| EP2258358A3 (en) | 2005-08-26 | 2011-09-07 | Braincells, Inc. | Neurogenesis with acetylcholinesterase inhibitor |
| WO2007036732A1 (en) | 2005-09-30 | 2007-04-05 | Astrazeneca Ab | Imidazo [1,2-a] pyridine having anti-cell-proliferation activity |
| EP1940389A2 (en) | 2005-10-21 | 2008-07-09 | Braincells, Inc. | Modulation of neurogenesis by pde inhibition |
| US20070112017A1 (en) | 2005-10-31 | 2007-05-17 | Braincells, Inc. | Gaba receptor mediated modulation of neurogenesis |
| US7705009B2 (en) | 2005-11-22 | 2010-04-27 | Hoffman-La Roche Inc. | 4-aminopyrimidine-5-thione derivatives |
| FR2894746B1 (en) * | 2005-12-09 | 2008-06-13 | Ipanema Technologies Sa | METHOD AND DEVICE FOR REMOTELY CONTROLLING CONGESTION OF MESH FLOWS IN A PACKET MODE TELECOMMUNICATION NETWORK |
| DE102005062742A1 (en) * | 2005-12-22 | 2007-06-28 | Bayer Schering Pharma Ag | New sulfoximine-substituted pyrimidines useful for treating e.g. diseases caused by inflammatory, allergic or proliferative processes, oncological diseases, cancer, eye, autoimmune and neurodegerative diseases |
| EP1803723A1 (en) * | 2006-01-03 | 2007-07-04 | Bayer Schering Pharma Aktiengesellschaft | (2,4,9-triaza-1(2,4)-pyrimidina-3(1,3)-benzenacyclononaphan-3^4-yl)-sulfoximide derivatives as selective inhibitors of the aurora kinase for the treatment of cancer |
| CA2642229C (en) | 2006-02-24 | 2015-05-12 | Rigel Pharmaceuticals, Inc. | Compositions and methods for inhibition of the jak pathway |
| US20100216734A1 (en) | 2006-03-08 | 2010-08-26 | Braincells, Inc. | Modulation of neurogenesis by nootropic agents |
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